Current World Literature
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Reference311 articles.
1. Long-term observational, non-randomized study of enzyme replacement therapy in late-onset glycogenosis type II.;Bembi;J Inherit Metab Dis,2010
2. SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder.;Cantagrel;Cell,2010
3. Guanosine diphosphate-mannose: GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations.;Dupre;J Med Genet,2010
4. Metabolic manipulation of glycosylation disorders in humans and animal models Review.;Freeze;Semin Cell Develop Biol,2010
5. Plasma N-Glycan Profiling by Mass Spectrometry for Congenital Disorders of Glycosylation Type II.;Guillard;Clin Chem,2011
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